GoodSense Artifical Tears
- Product NDC
- 50804-017
- 11-digit product format
- 508040017
- Labeler code
- 50804
- Product ID
- 50804-017_ec31a216-6f23-420a-962b-b705633f8232
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Polyvinyl alcohol, and Povidone
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Geiss, Destin and Dunn, Inc.
- Application
- part349
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-04-04
- Marketing end
- 0000-00-00
- Substance
- POLYVINYL ALCOHOL; POVIDONE
- Active strength
- 0 g/mL; g/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50804-017-05 | GoodSense Artifical Tears | 1 in 1 PACKAGE | SOLUTION/ DROPS | 1 | | 1 |
| 50804-017-05 | GoodSense Artifical Tears | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50804-017 | GOODSENSE ARTIFICAL TEARS (POLYVINYL ALCOHOL, AND POVIDONE) SOLUTION/ DROPS [GEISS, DESTIN AND DUNN, INC.] | 1 | Legacy NDC, 2 package rows | 20160405_f3ac9afa-e020-4fe6-98c6-04d44c86a8ba.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50804-017-05 | 50804001705 | 1 in 1 PACKAGE | Historical |